Clinical device trial and Medical Regulations specialist Clinius is a device CRO with main focus on clinical trials and regulatory consulting. We support companies in the healthcare and well-being industry in understanding the needs of customers as well as meeting the regulatory requirements (MDR/IVDR). We have more than 20 years experience with supporting device development. Our key services: - MDD to MDR transition - Documentation for Medical CE-marking - ISO 13485 quality management systems - Pre-audits - Clinical device trials - Clinical evaluations - Training